Course description
This course offers a practical understanding of the European regulatory requirements applicable to medical device software, including a detailed overview of the Medical Device Regulation.
Delegates who participate will obtain access to an additional two hours of digital content on cyber security worth £200, comprising of pre-recorded video lectures, quizzes and downloadable presentations. In addition, delegates will be offered a place for themselves or a colleague on our online academy: Navigating the Regulations for Health Apps and Medical Device Software, taking place in early 2020.
Do you work at this organisation and want to update this page?
Is there out-of-date information about your organisation or courses published here? Fill out this form to get in touch with us.
Suitability - Who should attend?
The course covers software-only products, hardware product with embedded software, health apps and medical device software and is suitable for professionals in the following roles:
- Project and Product Management
- Software Architects
- Designers and Developers
- Research & Development Management
- Requirements Engineers
- Verification, Validation and Clinical Evaluation Specialists
- Usability Experts
- Cybersecurity Experts
- Risk Management Moderators
- Quality and Regulatory Specialists
Why choose PTI
On average, delegates of their online academies said:
Quality of content:
4/5
85% had applied content during the course to their role
Delivery rating:
4/5
Expenses
£1,595